MATREC provides researchers with the opportunity to test manufacturing protocols in a controlled, pre-GMP environment. Once your team has:

• Completed cGMP training
• Had standard operating procedures (SOPs) reviewed by MATREC staff

You can access the cleanroom to refine production workflows, accelerating the transition to full GMP compliance for clinical applications.

Optimize your biomanufacturing process before scaling to GMP facilities. Contact us for details.